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Biopsy Punch 2901-117L

by Sontec Instruments, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 23 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00192896123380 UDI-DI Date11 May 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Biopsy Punch
Generic Name
Skin-coring punch, reusable
Model / Ref / Catalog
2901-117L
Primary DI / UDI-DI
00192896123380
510(k) Number
FDA Product Code
GEI
GMDN Term
Skin-coring punch, reusable
Device Class
Class II
Regulation Number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilization Method
Dry Heat Sterilization
Size
Length — 450 Millimeter
Outer Diameter — 5.0 Millimeter

Related devices

Cleared under the same submission (K102921)

Show all (12)

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Properties

  • Prescription Use
  • Lot / Batch Number

Other properties (12)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No